LKB1 (STK11) (NM_000455) Human 3' UTR Clone

Specifications

Product Data
Product Name	LKB1 (STK11) (NM_000455) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	hLKB1; LKB1; PJS
ACCN	NM_000455
Insert Size	885 bp
Sequence Data	Insert Sequence (showhide) >SC210625 3’UTR clone of NM_000455 The sequence shown below is from the reference sequence of NM_000455. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGCCGGCTGTCGGCCTGCAAGCAGCAGTGAGGCTGGCCGCCTGCAGCCCGTGTCCAGGAGCCCCGCCAG GTGCCCGCGCCAGGCCCTCAGTCTTCCTGCCGGTTCCGCCCGCCCTCCCGGAGAGGTGGCCGCCATGCT TCTGTGCCGACCACGCCCCAGGACCTCCGGAGCGCCCTGCAGGGCCGGGCAGGGGGACAGCAGGGACCG GGCGCAGCCCTCCCCCCTCGGCCGCCCGGCAGTGCACGCGGCTTGTTGACTTCGCAGCCCCGGGCGGAG CCTTCCCGGGCGGGCGTGGGAGGAGGGAGGCGGCCTCCATGCACTTTATGTGGAGACTACTGGCCCCGC CCGTGGCCTCGTGCTCCGCAGGGCGCCCAGCGCCGTCCGGCGGCCCCGCCGCAGACCAGCTGGCGGGTG TGGAGACCAGGCTCCTGACCCCGCCATGCATGCAGCGCCACCTGGAAGCCGCGCGGCCGCTTTGGTTTT TTGTTTGGTTGGTTCCATTTTCTTTTTTTCTTTTTTTTTTTAAGAAAAAATAAAAGGTGGATTTGAGCT GTGGCTGTGAGGGGTGTTTGGGAGCTGCTGGGTGGCAGGGGGGCTGTGGGGTCGGGCTCACGTCGCGGC CGCCTTTGCGCTCTCGGGTCACCCTGCTTTGGCGGCCCGGCCGGAGGGCAGGACCCTCACCTCTCCCCC AAGGCCACTGCGCTCTTGGGACCCCAGAGAAAACCCGGAGCAAGCAGGAGTGTGCGGTCAATATTTATA TCATCCAGAAAAGAAAAACACGAGAAACGCCATCGCGGGATGGTGCAGACGCGGCGGGGACTCGGAGGG TGCCGTGCGGGCGAGGCCGCCCAAATTTGGCAATAAATAAAGCTTGGGAAGCTTGGA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_000455.5
Synonyms	hLKB1; LKB1; PJS
Summary	This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq, Jul 2008]
Locus ID	6794
MW	32.1

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